Oligoasthenozoospermia with rare karyotypeÜlkü Özbey, Hüseyin YüceFirat University Faculty of Medicine, Department of Medical Biology and Genetics, Elazig
In a couple who had been investigated because of infertility, oligo-asthenozoospermia was diagnosed in man, by sperm analysis. Cytogenetic analyse, the karyotype of man was exhibited as 46,XY, t(9;15) (pter ›q21.1: : q11.1›qter), der(9)(ptel›q21.1), whereas his wife's was 46,XX. To our knowlodge, this is the first case, which was determined by conventional cytogenetic techniques, reported in the literature associated with severe male infertility. The degree of the efficiency of this rare karyotype on abortions and genetic counselling period that includes evaluating the view of unbalanced segragations of this karyotype was argued based on the literature. Keywords: Male infertility, chromosomal translocation, Oligoasthenozoospermia, meiotic pattern
Nadir karyotipli oligoastenozoospermiÜlkü Özbey, Hüseyin YüceFırat Üniversitesi Tıp Fakültesi, Tıbbi Biyoloji ve Genetik Anabilim Dalı, Elazığ
Anahtar Kelimeler: Erkek infertilitesi, kromozomal translokasyon, oligoastenozoospermi, mayotik patern
Ülkü Özbey, Hüseyin Yüce. Oligoasthenozoospermia with rare karyotype. Medeniyet Med J. 2007; 22(4): 158-160
Corresponding Author: Ülkü Özbey, Türkiye |
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